Abstract | BACKGROUND: OBJECTIVE: To examine the modulation of fibrogenesis by CDDO in explanted fibroblasts, skin organ cultures and murine models of scleroderma. MATERIAL AND METHODS: The effects of CDDO on experimental fibrosis induced by bleomycin injection or by overexpression of constitutively active type I TGF-β receptor (TgfbR1ca) were evaluated. Modulation of fibrotic gene expression was examined in human skin organ cultures. To delineate the mechanisms underlying the antifibrotic effects of CDDO, explanted skin fibroblasts cultured in two-dimensional monolayers or in three-dimensional full-thickness human skin equivalents were studied. RESULTS:
CDDO significantly ameliorated dermal fibrosis in two complementary mouse models of scleroderma, as well as in human skin organ cultures and in three-dimensional human skin equivalents. In two-dimensional monolayer cultures of explanted normal fibroblasts, CDDO abrogated fibrogenic responses induced by TGF-β. These CDDO effects occurred via disruption of Smad-dependent transcription and were associated with inhibition of Akt activation. In scleroderma fibroblasts, CDDO attenuated the elevated synthesis of collagen. Remarkably, the in vitro antifibrotic effects of CDDO were independent of PPAR-γ. CONCLUSIONS: The PPAR-γ agonist triterpenoid CDDO attenuates fibrogenesis by antagonistically targeting canonical TGF-β/Smad and Akt signalling in a PPAR-γ-independent manner. These findings identify this synthetic triterpenoid as a potential new therapy for the control of fibrosis.
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Authors | Jun Wei, Hongyan Zhu, Kazuhiro Komura, Gabriel Lord, Michal Tomcik, Wenxia Wang, Sruthi Doniparthi, Zenshiro Tamaki, Monique Hinchcliff, Joerg H W Distler, John Varga |
Journal | Annals of the rheumatic diseases
(Ann Rheum Dis)
Vol. 73
Issue 2
Pg. 446-54
(Feb 2014)
ISSN: 1468-2060 [Electronic] England |
PMID | 23515440
(Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
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Chemical References |
- 2-cyano-3,12-dioxoolean-1,9-dien-28-oic acid
- PPAR gamma
- Transforming Growth Factor beta
- Oleanolic Acid
- Collagen
- Proto-Oncogene Proteins c-akt
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Topics |
- Adipogenesis
(drug effects)
- Adult
- Animals
- Biopsy
- Cells, Cultured
- Collagen
(biosynthesis)
- Disease Models, Animal
- Drug Evaluation, Preclinical
(methods)
- Female
- Fibroblasts
(drug effects, metabolism)
- Fibrosis
- Humans
- Infant, Newborn
- Mice
- Mice, Inbred C57BL
- Oleanolic Acid
(analogs & derivatives, pharmacology, therapeutic use)
- Organ Culture Techniques
- PPAR gamma
(agonists, metabolism, physiology)
- Proto-Oncogene Proteins c-akt
(antagonists & inhibitors, metabolism)
- Scleroderma, Systemic
(drug therapy, metabolism, pathology)
- Signal Transduction
(drug effects)
- Skin
(drug effects, pathology)
- Transforming Growth Factor beta
(antagonists & inhibitors, pharmacology)
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